# Compex Technologies, Inc.

- Location (FDA's records): New Brighton, MN
- FDA decisions: 2 (2005–2007): 2 510(k) clearances
- Product codes: IPF (1), GZJ (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Staodyne, Inc.: 2 (https://510kreport.com/company/staodyne)
- Axelgaard Mfg. Co., Ltd.: 2 (https://510kreport.com/company/axelgaard-mfg)
- Medical Devices, Inc.: 1 (https://510kreport.com/company/medical-devices)
- American Imex: 1 (https://510kreport.com/company/american-imex)

## Firms that cite its devices most
- Bio-Medical Research, Ltd.: 2 (https://510kreport.com/company/bio-medical-research)
- Flowaid Medical Technologies, Corp: 1 (https://510kreport.com/company/flowaid-medical-technologies)
- Empi: 1 (https://510kreport.com/company/empi)
- Actegy, Ltd.: 1 (https://510kreport.com/company/actegy)
- Vision Quest Industries, Inc.: 1 (https://510kreport.com/company/vision-quest-industries)
- Hollywog, LLC: 1 (https://510kreport.com/company/hollywog)

## Its most-cited devices
- K050046: Rehabilicare IF 3 Wave Interferential Stimulator System, Model 7110S (2005), cited by 4
- K061516: Staodyn Max Preset, Model 4470 (2007), cited by 3

## Recent decisions
- K061516: Staodyn Max Preset, Model 4470 (Feb 6, 2007)
- K050046: Rehabilicare IF 3 Wave Interferential Stimulator System, Model 7110S (Apr 13, 2005)

Source page: https://510kreport.com/company/compex-technologies